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MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2018-02, Vol.56 (3), p.502-511

2018

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A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

European journal of medical genetics, 2018-04, Vol.61 (4), p.197-203

2018

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TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

Biochemical and biophysical research communications, 2015-03, Vol.459 (1), p.166-171

2015

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Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

International Heart Journal, 2017, Vol.58(4), pp.521-529

2017

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ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

Heart and vessels, 2018-07, Vol.33 (7), p.722-732

2018

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GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

Biochemical and biophysical research communications, 2013-10, Vol.439 (4), p.591-596

2013

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A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

International journal of molecular medicine, 2015-02, Vol.35 (2), p.478-486

2015

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GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

International journal of molecular medicine, 2014-11, Vol.34 (5), p.1315-1322

2014

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CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2017, Vol.55 (9), p.1417

2017

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HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

European journal of medical genetics, 2019-09, Vol.62 (9), p.103540-103540, Article 103540

2019

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CASZ1 loss-of-function mutation associated with congenital heart disease

Gene, 2016-12, Vol.595 (1), p.62-68

2016

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A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

G3 : genes - genomes - genetics, 2016-04, Vol.6 (4), p.987-992

2016

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GATA5 loss-of-function mutation in familial dilated cardiomyopathy

International journal of molecular medicine, 2015-03, Vol.35 (3), p.763-770

2015

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PITX2 loss-of-function mutation contributes to tetralogy of Fallot

Gene, 2016-02, Vol.577 (2), p.258-264

2016

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GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve

International journal of molecular medicine, 2014-05, Vol.33 (5), p.1219-1226

2014

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HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2016-07, Vol.54 (7), p.1161-1167

2016

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NKX2-6 mutation predisposes to familial atrial fibrillation

International journal of molecular medicine, 2014-12, Vol.34 (6), p.1581-1590

2014

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A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect

Pediatric cardiology, 2015-03, Vol.36 (3), p.646-656

2015

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Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

Molecular medicine reports, 2017-04, Vol.15 (4), p.2247-2254

2017

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TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

Molecular medicine reports, 2016-05, Vol.13 (5), p.4349-4356

2016

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Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease

European journal of medical genetics, 2014-10, Vol.57 (10), p.579-586

2014

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PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

Clinics (São Paulo, Brazil), 2014-01, Vol.69 (1), p.15-22

2014

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Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy

Molecular medicine reports, 2015-09, Vol.12 (3), p.3718-3724

2015

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TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

International journal of medical sciences, 2017-01, Vol.14 (4), p.323-332

2017

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MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

CASZ1 loss-of-function mutation associated with congenital heart disease

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

GATA5 loss-of-function mutation in familial dilated cardiomyopathy

PITX2 loss-of-function mutation contributes to tetralogy of Fallot

GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve

HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy

NKX2-6 mutation predisposes to familial atrial fibrillation

A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect

Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease

PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

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